Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP134975.RABcd9yh_e9SbvHN3DPIszvdGjDRUwlV-nWo1n0adNNeo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP134975.RABcd9yh_e9SbvHN3DPIszvdGjDRUwlV-nWo1n0adNNeo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP134975.RABcd9yh_e9SbvHN3DPIszvdGjDRUwlV-nWo1n0adNNeo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP134975.RABcd9yh_e9SbvHN3DPIszvdGjDRUwlV-nWo1n0adNNeo130_provenance.
- NP134975.RABcd9yh_e9SbvHN3DPIszvdGjDRUwlV-nWo1n0adNNeo130_assertion description "[Results describe the characteristic features of myosclerosis myopathy with a homozygous collagen type 6A2 mutation responsible for a peculiar pattern of collagen VI defects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP134975.RABcd9yh_e9SbvHN3DPIszvdGjDRUwlV-nWo1n0adNNeo130_provenance.
- NP134975.RABcd9yh_e9SbvHN3DPIszvdGjDRUwlV-nWo1n0adNNeo130_assertion evidence source_evidence_literature NP134975.RABcd9yh_e9SbvHN3DPIszvdGjDRUwlV-nWo1n0adNNeo130_provenance.
- NP134975.RABcd9yh_e9SbvHN3DPIszvdGjDRUwlV-nWo1n0adNNeo130_assertion SIO_000772 18852439 NP134975.RABcd9yh_e9SbvHN3DPIszvdGjDRUwlV-nWo1n0adNNeo130_provenance.
- NP134975.RABcd9yh_e9SbvHN3DPIszvdGjDRUwlV-nWo1n0adNNeo130_assertion wasDerivedFrom lhgdn-20090331 NP134975.RABcd9yh_e9SbvHN3DPIszvdGjDRUwlV-nWo1n0adNNeo130_provenance.
- NP134975.RABcd9yh_e9SbvHN3DPIszvdGjDRUwlV-nWo1n0adNNeo130_assertion wasGeneratedBy ECO_0000203 NP134975.RABcd9yh_e9SbvHN3DPIszvdGjDRUwlV-nWo1n0adNNeo130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP134975.RABcd9yh_e9SbvHN3DPIszvdGjDRUwlV-nWo1n0adNNeo130_provenance.